Nkx2.7 is a conserved regulator of craniofacial development

Nkx2.7 is a conserved regulator of craniofacial development

Abstract Craniofacial malformations arise from developmental defects in the head, face, and neck with phenotypes such as 22q11.2 deletion syndrome illustrating a developmental link between cardiovascular and craniofacial morphogenesis. NKX2-5 is a key cardiac transcription factor associated with con...

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Main Authors: Caitlin Ford, Carmen de Sena-Tomás, Tint Tha Ra Wun, Angelika G. Aleman, Uday Rangaswamy, Jake Leyhr, María I. Nuñez, Cynthia Zehui Gao, Hieu T. Nim, Michael See, Ugo Coppola, Joshua S. Waxman, Mirana Ramialison, Tatjana Haitina, Joanna Smeeton, Remo Sanges, Kimara L. Targoff
Format: Article
Language:English
Published: Nature Portfolio 2025-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-58821-3
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https://doi.org/10.1038/s41467-025-58821-3

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